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Catalog Number:
40188
CAS Number:
28611-39-4
4-(Dimethylamino)phenylboronic acid
Purity:
97 - 105 % (Assay by titration)
Synonym(s):
4-(Dimethylamino)benzeneboronic acid
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Product Information

4-(Dimethylamino)phenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its unique properties enable it to participate in Suzuki-Miyaura cross-coupling reactions, which are pivotal in constructing complex organic molecules. Researchers and industry professionals often leverage this compound for its effectiveness in drug discovery and development, particularly in the synthesis of biologically active compounds.

In addition to its role in synthetic chemistry, 4-(Dimethylamino)phenylboronic acid is also valuable in the field of materials science, where it can be used to modify surfaces and enhance the properties of polymers. Its compatibility with various functional groups allows for diverse applications, making it a preferred choice for chemists looking to innovate in their research. With its proven track record and broad applicability, this compound stands out as a key player in advancing chemical research and development.

Synonyms
4-(Dimethylamino)benzeneboronic acid
CAS Number
28611-39-4
Purity
97 - 105 % (Assay by titration)
Molecular Formula
C8H12BNO2
Molecular Weight
165.0
MDL Number
MFCD01074642
PubChem ID
2734344
Melting Point
227 °C (Lit.)
Appearance
White to orange crystalline powder
Conditions
Store at ≤ -4 °C
General Information
Synonyms
4-(Dimethylamino)benzeneboronic acid
CAS Number
28611-39-4
Purity
97 - 105 % (Assay by titration)
Molecular Formula
C8H12BNO2
Molecular Weight
165.0
MDL Number
MFCD01074642
PubChem ID
2734344
Melting Point
227 °C (Lit.)
Appearance
White to orange crystalline powder
Conditions
Store at ≤ -4 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-(Dimethylamino)phenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting cancer and diabetes.
  • Bioconjugation: It is used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing the effectiveness of drug delivery systems.
  • Sensor Technology: The compound is employed in the fabrication of sensors for detecting biomolecules, making it valuable in medical diagnostics and environmental monitoring.
  • Organic Electronics: Its properties make it suitable for use in organic electronic materials, contributing to advancements in flexible displays and solar cells.
  • Catalysis: The compound acts as a catalyst in various organic reactions, improving reaction rates and selectivity, which is crucial for efficient chemical manufacturing.

Citations